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By Felipe P. D. Lopes, Jr. dos Santos, Sergio N. Monteiro, Frederico M. Margem

"Natural fibers are gaining attention as a class of low cost, biodegradable and renewable materials that also exhibit some interesting properties for specific applications. In particular, the incorporation of some natural fibers in polymeric matrix composites is nowadays providing opportunity of manufacturing a variety of industrial items, for instance automobile interior components. Among these fibers, ramie (Boehmeria nivea) is one of the least investigated and only recently was studied as polymeric composite reinforcement. Therefore, the objective of this work was to evaluate the possibility of ramie waste reinforced polyester composites to replace conventional building materials, such as plywood, plastic boards and gypsum panels in terms of a cost-benefit analysis.IntroductionThere is a growing concern over the environmental questions that are presently affecting our society in a global sale such as climate changes and generalized pollution. Among the solutions for these questions, the replacement of energy intensive materials, especially those long term degradable such as the synthetic fibers, is already being considered [1]. As a consequence, the past decades have witnessed an increase in research devoted to new biodegradable materials obtained from natural resources mainly the biomass. Important examples are the renewable natural fibers as well as composites incorporated with them [2,3]. In addition to their friendly status with respect to the environment, well know natural fibers like jute, sisal, wood, coir, hemp and flax are relatively low cost and recyclable. In recent works [4,5], the use of these cultivated and abundant lignocellulosic fibers was investigated as the reinforcement phase in polymeric composites.Other less know lignocellulosic fibers have also been recently investigated [6,7]. These are fibers that likewise show a potential of incorporation into the polymeric matrix of composite materials. Most of these less know fibers are typical of tropical regions and, in principle, their application in industrialized composites would represent job opportunities for developing countries in Africa, South Asia and Latin America."

Jan 1, 2008

By Kerri-Ann Hue, Kerry Hasapidis, Ken Babcock, Patrick O'Hagan

"Metallic nanoparticles exhibit properties that are significantly different from individual atoms or bulk materials. Their applications are diverse and have varying uses in areas such as cancer treatment, biochemical sensors, nanoelectronics, and drug delivery. For each application extensive characterization must be performed in order to probe the unique properties of these nanoparticles. In this study, ultra-high resolution mass sensors consisting of MEMs-fabricated, suspended microchannel resonators (SMRs) were used to determine the size and concentration of metallic nanoparticles. With femtogram (10- 15 g) mass resolution, ultra-high resolution mass sensors can weigh individual particles suspended in fluid, and so measure their mass, density, and size. Particle size analysis with these sensors provides excellent accuracy and resolution compared to mature technologies such as light scattering. This technique also provides quantitative information via the ability count particles.IntroductionThe unique electronic, chemical, and optical properties associated with nanoparticles vary with their size, shape, and composition[ 1-4]. These properties are attributed to increased surface area and nanosized mean free path of electrons to the particle surface. Nanoparticle colloidal solutions have been prepared and are commercially available. In recent years, noble metals such as gold, copper, and silver have been extensively researched[5-7]. In order to tailor the optical, electronic, and electrical properties of nanoparticles, size and shape must be controlled. For many applications a monodisperse colloidal solution is ideal. Methods of size characterization include Transmission Electron Microscopy (TEM), Dynamic Light Scattering (DLS), and Electrophoretic Mobility Measurements to name a few[6, 8]. Although TEM can provide shape and size distributions, sample preparation requires that samples be dried on a metal grid and cannot be analyzed in solution. DLS uses curve fitting algorithms that while useful for determining mean particle diameters are not ideal for polydisperse colloidal solutions. New technologies are therefore needed to accurately determine the particle size distributions of metallic nanoparticles."

Jan 1, 2011

By Ludy C. Motta, Denise C. O. Nascimento, Sergio N. Monteiro

"Natural cellulose-based fibers are nowadays of growing interest for modern industrial composites. Relatively unknown fibers like piassava, curaua and gourde have shown promising behavior as reinforcement of polymeric composites. However, the hydrophilic characteristics of the natural fibers impair its adhesion to the normally hydrophobic polymeric matrix. Surface treatments can, in principle, improve this adhesion and the fiber/matrix interfacial strength. In this paper, the effect of alkali treatment of the surface of piassava (Atallea funifera) waste fibers was investigated in terms of the change in strength of epoxy composites reinforced with these waste fibers.IntroductionThe consequences of global warming and the increase in the price of petroleum are motivating the use of natural materials as substitute for energy intensive synthetic materials [1]. In particular, natural fibers obtained both, from cultivated plants such as jute, sisal, hemp and flax as well as from industrial waste such as sugar come bagasse and coir, are being considered to replace synthetic glass fibers [2,3]. These natural fibers, also known as lignocellulosic fibers, present the comparative advantages of being renewable, recyclable and biodegradable. Moreover, lignocellulosic fibers require less amount of processing energy and are neutral with respect to CO2 emission, which causes the atmospheric greenhouse effect responsible for the global warming [4]. Low cost is another important economical advantage of the natural fibers over the synthetic ones and the application of lignocellulosic is also associated with a lower wear of processing equipment and better finishing of molded components [5]. Moreover, for some fibers, properties such as the mechanical strength and impact resistance can be superiors to the corresponding properties of synthetic glass fiber [6]. The characteristics and properties of several lignocellulosic fibers are, nowadays being extensively discussed in the literature. It is beyond the scope of this work to comment on the hundreds of papers dealing with this subject. However, there are still less known fibers with great potential as engineering material that deserves investigation."

Jan 1, 2008

By Honorio Oliveros Gómez, Oscar Jaime B. Restrepo

"Colombia produces nine tons of electronic waste per year and there are approximately 60 tons accumulation generated in the last nine years. This work aims to establish a general methodology in the laboratory to recover gold, silver and platinum group present in electronic waste, also explore other forms of recovery of metals contained in electronic waste. We selected seven types of electronic cards present in the computers, which have their parent desoldering electronic components. Initially, we characterized the components of the cards through X-ray diffraction and SEM, to identify the metal species and composition. Tests were conducted laboratory hydrometallurgical recovery of metals. This paper proposes a methodology for laboratory-scale work.INTRODUCTIONColombia produces nine tonnes of electronic waste per year and build there in about 60 tons generated in the last 9 years [1], Computers, TVs, audio equipment, monitors, cell phones, remote controls, printers and operated toys battery, among others are part of this inventory, which mostly comes to landfills, because the lack of legislation to control the final destination of waste electrical and electronic equipment, and lack of efficient technologies to recover materials [2]. Under these circumstances which have environmental implications, technological and economic recovery is essential metals present in the electronic cards of computers, by hydrometallurgical with subsequent base metal electrodeposition [3]. Pyrometallurgical route is discarded by major implications for economic and environmental [4]. Recovery From this perspective, the determination of the metal fraction and the relationship between the different metals, using the SEM characterization techniques - BSE and XRD is indispensable [5] It follows with electrolytic dissociation processes in the leaching and electrodeposition [6], and unit operations in the laboratory to carry out successfully these processes on a larger scale. Were randomly selected computer twenty-four postcards for nine types of cards have different functions in the computer, which, through the absorption desoldering technique, they broke the resistance (thermal, surface, photoresist, power), capacitors (ceramic, electrolytic), diodes (silicon, germanium, high frequency), transistor (NPN, PNP), processors, integrated (high, medium and low frequency), the RAM card and pin parallel port serial"

Jan 1, 2011

By Guodong Lai, Shixing Wang, Lijuan Chu, Jinhui Peng, Zebiao Zhang

"The beneficiation of poor manganese ores containing phosphate gangue is very difficult by conventional processes, because of the similarities in the physico-chemical properties of the constituent minerals. The shaking table gravity concentration process and concentrated strong acid selective intensified leaching process were used for dephosphorisation of Yunnan manganese ore. The leaching process was effective. The effects of intensified leaching time, solid-liquid ratio and particle size were investigated. The relevant leaching factors were optimized as -0.125+0.088 mm particle size with 68% nitric acid for 24 h when using a solid-liquid ratio of 1:1 at room temperature and atmospheric pressure. Under these conditions, the P/Mn ratio was reduced from 0.0107 to 0.0056, and the grade of manganese was increased from 12.32% to 42.76%. The dissolution of manganese during leaching was negligible.IntroductionManganese and its compounds are widely used in the iron and steel industry as deoxidation and desulfurization agents and as alloying additives [1-2]. Because of the increase in demand, low grade refractory manganese ores are becoming a new source. Many Chinese manganese ores are high in phosphorus, which cannot be used directly for metallurgical purposes. This occurs because phosphorus enters into the metal phase during smelting and its presence sharply deteriorates the mechanical properties of the metal [3-4].Kanungo and Sant [3] investigated the dephosphorization of phosphorus-rich manganese ores by selective leaching with dilute hydrochloric acid. They observed that leaching with dilute hydrochloric acid (0.1-0.6M) could reduce the phosphorus contents to the specified limit of 0.12%. Ye [5] investigated dephosphorization of high-phosphorus manganese ore of the Huayuan type. Using high intensity magnetic separation, roasting and leaching with acid for dephosphorization, as used in the industry, a 40.15% manganese concentrate with a P/Mn ratio of 0.0037 was obtained. Yimin [6] investigated magnetic separation followed by inverse flotation of high-phosphorus manganese ore, and found that the P/Mn ratio could be reduced from 0.046 to 0.002."

Jan 1, 2012

By J. B. Vander Sande, I. G. Solórzano, B. S. You, P. M. Jardim, W. W. Park

"Alloys with six different compositions in the system Mg-Ca-Zn were produced by melt spinning. The aging behavior of alloys was investigated by measuring the changes in microhardness after isochronal aging and the microstructure was analyzed by means of transmission electron microscopy (TEM), energy dispersive X-ray spectrometry (EDS), scanning transmission electron microscopy (STEM) and scanning electron microscopy (SEM). All six compositions in the as-solidified condition show a difference in microstructure between the wheel contact side (zone A) and the free surface side (zone B) as a result of the differences in the solidification rate across the ribbons. One of the alloys (Mg-l.5wt%Ca-6wt%Zn) was chosen to be more deeply investigated in this work as it exhibited grain boundary films and an age hardening behavior was produced in that alloy.IntroductionMagnesium is the lightest of all the commonly used metals, and very attractive for applications in transportation. It also has a number of other desirable features, including good ductility, better damping characteristics than aluminum, and excellent castability. However, there are some negative features, such as high reactivity in the molten state, inferior fatigue and creep resistance as compared to aluminum, poor corrosion resistance and high production cost.In recent years there has been a significant increase in magnesium use as a structural material. These structural applications include aerospace, automotive and nuclear industries as well as appliances and sporting goods (1 ). According to reports on Mg-Zn alloys, the addition of Zn (2) in magnesium increased strength. Also, since the maximum solubility of Zn in magnesium is 6.2wt%, a considerable amount of Zn can be retained in solid solution in magnesium alloys by rapid solidification. In addition, Ca is known (3) to be one of the most potent alloying elements for refining the microstructure and precipitates in magnesium alloys, and also to improve mechanical strength and corrosion resistance."

Jan 1, 2000

By Caisa Samuelsson, Sina Mostaghel, Theo Lehner

"Rönnskär smelter of Boliden Mineral AB, Sweden, is well known for recycling of base and precious metals. Slag from the electrical furnace is processed at the fuming plant to produce zinc clinker. The granulated slag is a by-product used as e.g. construction material. In this paper, influences of Al2O3 on mineralogy of the slag, which can affect its chemical and physical properties, are investigated. Different mixtures of Al2O3/fumed slag were prepared. Re-melting was carried out in a Thermo-Gravimetry (TG) furnace with an inert atmosphere. Scanning electron microscopy (SEM) and X-ray diffractometer (XRD) were then applied for the analyses. Investigations depict that addition of alumina to slag, results in an increase in the number of spinels and a transformation from iron rich to aluminum rich spinels. Anorthite (CaAl2Si2O8) will also be formed.IntroductionRönnskär smelter of Boliden Mineral AB is located in north of Sweden; the main products of this smelter are: Copper, Zinc clinker, Lead, Gold, and Silver, while sulphuric acid, liquid sulphuric dioxide, and Iron sand are some of the by-products. Reducing the energy consumption and decreasing the usage of finite natural resources are becoming more and more important for the Rönnskär smelter; this result in use of different recycling and scrap materials. Metal residues, from brass foundries, steel mills, and electronic scrap are recycled at Rönnskär smelter [1]. Most of the electronic scraps contain mixtures of various metals together with plastics and ceramics, which can affect the composition and properties of the slag considerably [2]. At the same time, treatment of slag and controlling its composition and properties are of much interest for Base Metals producers from different aspects. Composition of slag influences the physical properties such as: 1) Liquidus temperature [3-4] 2) Viscosity, which controls separation of valuable metals, especially copper by gravity separation [2] and also heat and mass transfer [5] 3) Electrical conductivity [6]."

Jan 1, 2008

By Yan Fu, Chuanlin Fan, Xiujing Zhai, Yongfeng Chang, Binchuan Li

"The mechanism of the selective chlorination of nickel and cobalt in reduced limonitic laterite was investigated. Reduced ores were obtained from the reduction roasting of a limonitic nickel laterite. The thermal decomposition of related chlorides and the selective chlorination of the reduced ore were carefully studied using Differential Thermal analysis - Thermogravimetry (DTA-TG), X-Ray Diffraction and chemical leaching methods. In the temperature range of 300 - 500 °C, aluminum chloride hexahydrate was chosen as chloride agent. During the selective chlorination, reduced ore was partly chlorinated by hydrogen chloride generated from the thermal decomposition of chloride agent. Then the oxydrolysis of ferrous chloride re-generated hydrogen chloride was used to further the chlorination. Finally, iron was mostly rejected as hematite, while nickel and cobalt were selectively chlorinated. More than 91 %Ni , 90%Co and about 4%Fe in the chlorinated ore was extracted using a water leaching method.IntroductionLimonitic nickel laterite is an important nickel reserve, which is rich in iron in the form of goethite and has low contents of magnesium, aluminum, silicon, and other elements. Goethite is the main nickel-bearing mineral in the laterite [1]. Nickel is generally present in goethite in three modes: (a) associated with amorphous or poorly crystalline goethite, (b) weakly adsorbed to the crystalline goethite surface, and ( c) as lattice substituents [2]. In addition, cobalt in limonite was found to be associated with a manganese phase rich also in nickel [3]. These results indicate that the extractions of nickel and cobalt are highly dependent upon the degree of the decomposition of the nickel, cobalt-bearing minerals.For the selective extraction of nickel and cobalt from limonitic laterite, the ore is usually processed by hydrometallurgical methods, including high pressure acid leaching (HPAL) [4] or reductive roasting - ammonia leaching (Caron process). However, there are still some disadvantages in these processes, such as the expense of autoclaves and scaling problems in HP AL [ 4, 5], and relatively low overall metal recovery, large energy and reagent requirements for the Caron process."

Jan 1, 2011

By A. V. Tarasov, S. D. Klushin

493 The most common method for minimizing the copper content of residual slag in the process of autogenous smelting of sulfide raw materials is treatment of molten slag in an electric furnace, with optional addition of solid reducing agents, such as coke, and/or sulfiding agents such as pyrite. A drawback of this technique is the fact that the final slag produced still contains 0.5% or more Cu. We have tested a method for treating molten slag obtained as a result of autogenous smelting by a gaseous mixture of sulfur dioxide and methane at a ratio of. SC:SO2 = 0.75 :1.0 in the presence of oxygen. Interaction reaction within the SO2-O2-CRi system proceeded at a high rate at 1373 to 1573 K to form reducing and sulfiding agents: H2S, S, COS, CO, CO2, H2, H2O. The gas mixture requirement was about 100 to 150 Nm3 per 1 tonne of slag. A decrease in the ferric iron concentration (Fe3+) from 10-15% down to 2-3% resulted in lower solubility of copper in slag, and agitation of the melt with gas stream accelerated. the separation of the sulfide phase and slag. Removal of copper from slag was performed in a pilot unit within the second V anyukov furnace zone where slag arrived with a copper content of 0.8-1.3%. The temperature of molten slag was maintained within 1523 to 1573 K. The copper content of the final slag was at a level of0.12 to 0.14%. The matte sent to converting was a mixture of bottom matte from the smelting zone and the slag treatment zone. It had a copper content of about 50 to 55%. Process gases from both furnace zones were combined and sent to the acid plant for sulfur recovery. This process was offered for commercial use at two copper smelters in Russia and CIS.

Jan 1, 2000

By Samson Adeosun, Sanmbo Balogun, David Esezobor

"In a typical year, approximately 1.7 million tons of residues and wastes are expected from Ajaokuta integrated steel plant, Nigeria. They will be generated mainly from sinter plant, blast furnace (BF), and basic oxygen furnace (BOF) operations and during rolling and finishing. The residues and wastes include slag, dust, sludge and slurries from gas cleaning, waste water, mill scales and other associated scraps. In this paper concepts for the utilization of residues and wastes in Ajaokuta Steel Plant where no reclamation routines have been provided for in the first and second phases of its project implementation is designed. The paper analyses the sources of the iron oxide wastes and evaluates the quantities expected from the main production facilities of the plant which include the two 312 m2 capacity sintering machines, the two 2000 m3 blast furnaces and two 130-T BOF (of the 2nd phase expansion of the Steel Plant). A reclamation routine designed for Ajaokuta residues and wastes is presented.IntroductionIn the steel industry, approximately 550kg of residues per ton of crude steel arise from the production processes and from pollution control facilities [1- 4]. These residues consist of slag, dusts and sludge, mill scale, spent pickle liquor, and other iron bearing materials. The main by – products generated in the steel industry are listed in Table I.Although major progress has been made in the recycling and use of some of these residues, particularly flue dust, blast furnace and steel making slag, yet a significant quantity are land filled or stockpiled. These unsightly stockpiles occupy valuable real estate and may become a source of environmental pollution if not otherwise disposed. In any case, the dumping option has become quite costly. For instance, one ton of iron ore costs between 28 and 34 US dollar, whereas as much as $20 per ton of steel produced is required to meet environmental compliance obligation in the USA [5, 6]."

Jan 1, 2008

By Wander. L. Vasconcelos, Virgínia. S. T. Ciminelli, Angela. M. F. Guimarães

"The present work was aimed at synthesizing nanostructured hybrid materials derived from the functionalization of smectite clays with ligands containing thiol (-SH) groups for application in cadmium adsorption processes. An in nature Brazilian bentonite was investigated. The modification route was based on the grafting reaction between hydroxyl groups present on clay surface and the hydrolyzable alkoxy group of the (3-mercaptopropyl)trimethoxysilane in dry toluene under reflux. The present work showed that the proposed modification route was effective for the grafting of the thiol groups in the clay structure. The thiol-functionalized bentonite samples showed average binding capacities 160% higher with respect to Cd2+ to those obtained with the ungrafted material. These results support a mechanism of adsorption involving primarily ion complexation by the thiol groups (specific) instead of cation exchange (unspecific). The proposed modification processes are suggested for the preparation of novel adsorbent materials with controlled selectivity and specificity and therefore with good potential for separation and pre-concentration purposes.IntroductionMany efforts have recently been devoted to the design and preparation of inorganic-organic nanomaterials because of their potential application in novel functional materials. The intercalation of organic species within the spaces between interlayers of inorganic layered crystals provides nanostructures consisting of alternating layers of inorganic and organic compound. The intercalation reactions occur by insertion of mobile guest species (neutral, molecules, or ions) into the accessible crystallographic-defined vacant sites located between the layers (interlayer spacing) of the layered host structure [1}.Silane coupling agents, used widely for the modification of silica surfaces, have also been employed more recently for modification of layered silicates [2,3,4,5]. Modification with organosilane involves grafting reactions by establishing covalent bonds between the reactive groups of the layer, normally hydroxyl groups, and silane molecules. These reactions can be restricted to the external surface (the basal spacing remains unchanged) or to the interlayer surface, in which case an interlayer expansion occurs. The resulting material can be defined as a hybrid material or, more specifically, functionalized inorganic layered material [1]."

Jan 1, 2008

By Chu Yong Cheng

The solvent extraction (SX) processes of the three pressure acid leach (PAL) nickel plants in Western Australia have been reviewed. The use of intermediate precipitation, solids/liquid separation and re-leach in the three W A nickel plants make these processes complicated and costly in capital and ?operation. The research work carried out by the SX group at the AJ Parker Cooperative Research Centre for Hydrometallurgy I CSIRO Minerals has led to the development of direct solvent extraction (DSX) processes to recover and purify nickel and cobalt from leach solutions. The simplicity of the process flowsheets and the expected savings in capital and operating costs are the major advantages of the new DSX processes over the reviewed processes. By using a new synergistic organic system in semi-continuous tests with a pilot plant leach solution (after iron precipitation) from BHP-BiIliton Stainless Steel Materials, the metal values (Ni and Co) together with zinc and copper were separated from the major impurities (Mn, Mg and Ca, together with Cl) in the first SX circuit. The co-extracted manganese, magnesium and' calcium were easily scrubbed out. After stripping, the metal values (Ni and Co) together with zinc and copper were concentrated, resulting in a much smaller second SX circuit and equipment in the down stream processes. The extraction and stripping kinetics of the metals with the new synergistic organic solution were very fast. The extraction and stripping almost reached steady state within 0.5 minutes. Semi-continuous test work with a synthetic leach solution, a cobalt pilot plant leach solution from Peko Rehabilitation Project Pty Ltd and a synthetic solution to simulate a concentrated laterite leach solution from BHP-Billiton Stainless Steel Materials showed that manganese, calcium, copper and zinc can be effectively and efficiently separated from nickel, cobalt and magnesium by extraction, scrubbing and stripping. This led to the development of another DSX process using D2EHPA to recover nickel and cobalt from leach solutions.

Jan 1, 2003

By Jian Pan, Zhen He, Deqing Zhu, Shouyan Yue

"The differences of raw material characteristic among six kind of iron concentrates and the influences on ballability were studied from the aspect of the size distribution, specific surface area and particles morphology. The results show that the specific surface area of iron concentrates has crucial influence on ballability, and the effective method of improving ballability for weak ballability iron concentrate has been found. It is of important guidance for Chinese steel mills to import and use iron concentrate from the whole world.IntroductionChina's steel industry has developed rapidly in recent years, crude steel production in 2011 is an unprecedented 683 million tons, which is almost half of the world crude steel production, and it is equivalent to the total sum production of the nations which rank at 2,3,4,5 and 6 in the world [1]. In order to match the development of steel industry, the blast furnaces are becoming larger and more modernization, therefore charging burden of higher quality is requested, and the reasonable blast furnace burden structure is more and more important, at the same time, for iron ore powder sintering process's continuous improvement and development, another method providing ""concentrate"" for blast fumace-pelletizing is also taken seriously. The grate-kiln method of pelletizing has achieved great development for its unique advantage, and in just a few years, there are over 60 rotary kiln production lines have built or being built in China, the sum of pellets has reached to more than 140 million [2, 3]. The rapidly growth of pelletizing yield demands diverse source of pellet, which include not only domestic magnetite concentrate, but also imported hematite which is high in iron and low in silicon. Usually the ratio of imported hematite concentrate increased gradually. The imported hematite concentrate has high grade and fine particle size (the content of -0.074 mm mostly higher than 90%), but the ballability of part of the concentrates is poor."

Jan 1, 2013

By E. Kuzeci, R. Kammel

"Lately various voltametric methods have gained increased attention as an analytic tool in hydrometallurgy. Voltammograms with mercury drop electrodes or glassy carbon electrodes provide information about the electrocrystallization of cathodic deposits and allow calculation of kinetic data by means of characteristic parameters like the peak potential and peak current and their variation with the voltage scanning rate.Cyclic voltammograms are also suitable for identification of reaction sequences. Voltammograms with carbon paste electroactive electrodes containing metal sulphide additions reveal information about the dissolution behavior. The stripping voltammetry can be applied to analyze metal ions and organic additives (e. g., thiourea) in extreme low concentration. Typical application of the various methods studied with microcomputer controlled measurement system are explained by examples selected from copper hydrometallurgy.IntroductionThe use of electroanalytical methods in metallurgical process control can be dated back to the starting period of industrial copper refining, when the deposition of the metal ions was followed electro-gravimetrically by weighing the electrode with deposits (1). The principles of metal deposition and dissolution have not changed but the methods to follow these phenomena were subjected to noticeable developments and especially the introduction of polarographic investigations by Heyrowsky (2) has greatly contributed to the progress in electro-analysis. A review about the fundamental work on the electrochemical kinetics in earlier time is compiled in a monograph of Vetter (2). With the steady improvements in the instrumental techniques, it is nowadays possible to apply several current and potential modulations for measurements with improved selectivity and sensibility. There is however, still a lack in theoretical interpretation of the data obtained. More theoretical information are already available for linear voltametric methods for systems where reduced as well as oxidized species are dissolved in the electrolyte (4, 5). Some recent investigations have also shown the reliability of these techniques to study electro-crystallization (6, 7). Main fields of the application in the hydro - and electro-metallurgy are:"

Jan 1, 1989

By Batric Pesic

A hydrometallurgical process for recovery of Zn and Mn from Bunker Hill Water Treatment Plant sludge was developed. The process is unique because it treats an unusual combination of metals, Zn and Mn. Another non-standard feature of the process is that leaching takes place with ~S04 in the presence of a reductant (SO2). Zn and Mn are recovered simultaneously by electrowinning, Zn on a cathode and Mn on an anode, as MnO2 The major purpose of the process is to detoxify the sludge by removing toxic heavy metals. The recovered metal values could be marketed to offset the overall costs of water and sludge processing. This work is presented in two separate parts, 1. Leaching and Solution Purification, and II. Electrowinning. This paper covers only the first part of the hydrometallurgical process: Leaching and Solution Purification. Initially, the paper briefly discusses the history of the pollution problem at the Bunker Hill Superfund Site, the origin of heavy metals in the mine waters, and the development and use of the water treatment plant. The leaching of sludge was examined as a function of the following parameters: constant vs. initial pH, initial vs. delayed addition of SO2, temperature, and pulp density. It was found that leaching with H2SO4 at pH 2.0 for 15 minutes (at 60°C), followed by S02 addition for another 15 minutes, could completely dissolve Zn and Mn. Solution purifIcation was done in three stages. In the first stage iron was removed by adjustment of pH (to pH 5.0) and oxidation offerrous to ferric iron (with H2O2). In the second stage, Cu and Cd were removed by Zn dust cementation. Finally, Co and Ni were precipitated with the organic reagents 1-2 nitroso-naphthol and nitroso, respectively. Electrowinning of Zn and Mn is discussed separately in Part II of this paper.

Jan 1, 1996

By Ragnhild E. Aune, Shahid Akhtar, Reza Beheshti

"The potential use of Black Dross (BD) as a raw material for the production of refractories, fluxing agents and glasses is the main motivation of the present study. Heat treatment experiments were carried out in Ar, and under reduced pressure (20 Pa), to evaluate the salt removal efficiency. The chemical composition of the BD after heat treatment was investigated by SEM-EDS and XRD analyses. Based on the present results, it is established that the salt starts to evaporate at ˜1273 K in Ar, and under reduced pressure. The salt removal efficiency in a 20 g sample was found to increase in both cases as a function of time and temperature. Moreover, in Ar the chlorine concentration was lowered to 0.3 wt% after heat treatment at 1523 K for 10 hours. Under reduced pressure, however, 0.2 wt% residual chlorine was obtained after 8 hours at 1473 K.IntroductionIt is believed that aluminum recycling in the near future will become the main route of aluminum production [1]. Black dross (BD) that is produced during this process contains, among other things, high amount of salts like NaCl and KCl [2, 3]. Almost 800,000 tons of BD is annually land filled in United States and this number continues to grow with the increase in aluminum recycling [2]. The BD should be dumped in controlled land field and it is costly procedure [4, 5].The water-soluble compounds in BD react with water or environmental humidity and release chlorides into the water and/or generate toxic gases such as H2, CH4, NH3 and H2 S [6-8]. In the Europe, BD is considered as toxic waste and its disposal as landfill is forbidden [8, 9]. After salt removal, the BD is considered to be non-hazardous and can be buried under ground [10].On the other hand, BD do also contains many relatively valuable compounds that may be changed in to useful materials as a result of further treatment [11, 12]"

Jan 1, 2012

By Baicheng Liu, Houfa Shen, Wensheng Li

"In order to understand the formation of macrosegregation in steel ingots, a mixture model has been developed which accounts for coupled mass, momentum, species, and energy transport to describe the sedimentation of free equiaxed grains during solidification. In this model, the mushy zone is divided into the slurry and porous regimes according to a solid packing fraction. Settling velocity of equiaxed grains in the slurry regime is given by an explicit expression. The solidification of a binary steel ingot (Fe-0.36wt.%C) with a two-dimensional geometry is numerically simulated. It is demonstrated that the predicted macrosegregation patterns agree to some extent with classical experimental results. Further refinement of this model is still necessary for realistically simulating steel ingot solidification.IntroductionModeling macrosegregation in steel ingots is still a challenging study, mainly due to the length scale of the products and the complexity of global multiphase transport phenomena coupled with microscopic solidification kinetics [l]. The thermal-solutal convection and the motion of equiaxed grains are the two main mechanisms responsible for macrosegregation. But there are few models that deal with the motion of equiaxed grains, which is confirmed as the main phenomenon that explains the negative macrosegregation along the centerline of large steel ingots [2]. A model which takes into account melt convection and grain sedimentation was first proposed by Beckermann and co-workers ([3], and references therein). More recently, similar multiphase solidification models with advanced nature have been presented by Wu and Ludwig [1,4] and Combeau and co-workers [5,6]. It is known that the application of these sophisticated models to steel ingot casting is at its beginning.In this paper, a solidification model based on continuum mixture approach, using much less sophisticated relations to obtain the settling velocity of free equiaxed grains, has been proposed in order to predict the macrosegregation in steel ingots. The model is applied to simulate the solidification of a binary steel ingot with a two-dimensional geometry, and preliminary modeling results are presented."

Jan 1, 2011

By T. A. George, David J. Sellmyer

"The concept of achieving a useful high-energy-product magnet through appropriate nanostructuring of known hard and soft phases has been tantalizing researchers since the idea was first proposed. The fabrication of exchange-coupled nanocomposite magnets faces several challenges including aligning the easy anisotropy axes of the hard-phase grains. Here we investigate experimentally two-phase nanostructures of hard Lio-ordered FePt and soft iron-rich/cc Fe(Pt). The Fe-Pt thin films were produced by epitaxial cosputtering onto MgO (001) single-crystal substrates which lead to strong (001) texturing. The measured hysteresis loops indicate nearly ideal exchange coupling. Excellent magnetic properties are obtained, with largest values of coercivity (51 kOe), saturation magnetization (1287 emu/ cm3, J, = 16.2 kG), and nominal maximum energy product (58 MGOe).1. IntroductionA key figure of merit for permanent magnets is the maximum energy product (BH)rrw.x. The achievable maximum energy product is determined by a magnet's saturation magnetization M, and its magnetic anisotropy. For example, it is well known that (BH)rrw.x :S 4n2M,2• In the past, record energy products have been the result of discovering new compounds with high values of magnetization and anisotropy. However, finding new compounds with better magnetic properties than the current record-holding magnet Nd2Fe14B has proven to be difficult. A different approach is to exploit the exchange coupling mechanism between known hard and soft magnetic phases to enhance the maximum energy product [1-5]. In such a composite system, high coercivity is achieved due to the anisotropy of the hard phase as well as a nanostructure which prohibits large-scale domain wall reversal mechanisms. Magnetization is enhanced by the soft phase and loop squareness results from texturing of the hard phase easy-axis as well as complete exchange coupling between the coexisting hard and soft grains."

Jan 1, 2012

By Guangchun Yao, Chuan Li, Hongjie Luo, Zhuokun Cao

"The expansion rate and collapse time of liquid aluminum foams are essential for the determination of operating time and quality of the resulting foam. In the present paper, liquid aluminum foams was fabricated by adding in TiH2 as blowing agent, and the variation of expansion rate with foaming time was non-contact detected by a laser distance measurer. The influence of different stabilizing agent and alloying elements was studied. The results show the fact that the fraction of stabilizing agent only perform little effects on the maximum expansion rate of liquid aluminum foams, while the influence of alloy elements are remarkable. The maximum expansion rate would increase much when Mg is added, and the liquid foam also collapse at a shorter time. Comparison was made between experimental results and mathematic calculations, which reveal the fact that it is the change of TiH2 decomposition responsible for the change.IntroductionMetal foams, combining light weight with other unique mechanical and physical properties, have gained wide interest and been developing fast during past few decades. However, manufacture of this new material is quite challenging since it involves simultaneous occurrence of gas, liquid and solid phase at high temperature [1-2].Quite some manufacture routes have been developed for manufacturing metal foams, and the structure and quality of resulting foam are remarkably improved during the last decades. However, most of the past works seems to be experiential, and because the lack of basic knowledge of foaming process, the start material is limited and the production technologies are far from reliable and reproducible.[3-4]In direct foaming process, decomposition of blowing agents, TiH2 for example, is the main force for foam expansion. The density and foam structure changes with time during the foaming process, so it is expected that foams of certain structure can be obtained by solidification of the liquid foam at a certain time [5-6]. However, the foaming process is weak in reproducibility and the influence of stabilization additives and alloying elements is unclear."

Jan 1, 2011

By Laura Garcia H, Juan Carlos Gonzalez Islas, Luis Garcia Lechuga, Pedro Alberto Ramirez Ortega

"Electrochemical studies were performed to silver recovery from industrial wastes (radiographic films) on litanium flat electrode using a filter press-type electrochemical reactor with vertical orientation (known as REOV-01), as counter electrode was used a mesh-type DSA. Voltammetric studies were employed to fmd the current range under which silver reduction occurs. Using chronopotentiometric studies with controlled current, homogeneous deposits were obtained on the surface of the Ti electrode, to a current of -210 mA during 120 minutes to a constant linear flow velocity of 15 Lmin-1 was achieved 97% of silver recovery from industrial wastes. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy studies corroborated the presence of silver on Ti flat electrode. In addition, the silver concentration in the solution after the experiments was 1 ppm below environmental requirements. This indicates the viability of a filter press-type electrochemical reactor with vertical orientation (REOV-01) for silver recovery from radiographic filmsIntroductionIn recent years, the industrial sector has shown an increase in the use of silver due to new applications in different areas. In sectors such as photography, the consumption of silver has declined as a result of the boom in digital photography. However, the use of silver in radiographic applications has not shown greater variation (47.16 Moz), as the image quality is essential for diagnosis in various fields, such as medicine. All the silver used in photographic applications is discarded completely (solid or in effluent). At the present, several countries have been involved in silver recovering from industrial wastes due to the economic value and environmental impact they represent. The main source of silver recovery is the wastes generated by the photographic sector. Various technologies have attempted to recover silver contained in these wastes. However, they have not fully satisfied the requirements of maximum recovery, nor environmental level (less than 5 ppm) of silver in effluents [1,2]."

Jan 1, 2014